Therapy Areas: Central Nervous System
GenSight Biologics Appoints Françoise de Craecker to its Board of Directors
17 May 2021 - - France-based biopharma company GenSight Biologics (Euronext: SIGHT) has appointed Françoise de Craecker to its board of directors, replacing Natalie Mount, the company said.

de Craecker is joining as an independent director.

In her last position, de Craecker led the EMEA (Europe, Middle East and Africa) region at AveXis, further acquired by Novartis. She built from scratch the multifunctional team launching Zolgensma, the first one-shot Gene Therapy for the treatment of Spinal Muscular Atrophy, in the EMEA region.

She paved the way for the approval, distribution, market access and commercialization, working with authorities on innovative funding pathways and early access. She also established a wide presence in the main European markets and a network of distributors in the Middle East and other European countries.

Prior to joining AveXis, de Craecker was leading European operations for Raptor Pharmaceuticals at the critical phase of a shift from R and D to commercialization of their lead product in Cystinosis.

Before that, she was part of the team launching the first Orphan Drug approved in Europe and took different positions of increasing responsibilities within Shire Human Genetics. She also led various strategic and operational teams, locally and globally for 14 years.

de Craecker holds a Master's in Science from the Faculty of Medicine of the University of Leuven (Belgium).

GenSight Biologics S.A. is a clinical-stage biopharma company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders.

GenSight Biologics' pipeline leverages two core technology platforms, the Mitochondrial Targeting Sequence and optogenetics, to help preserve or restore vision in patients suffering from blinding retinal diseases.

Using its gene therapy-based approach, GenSight Biologics' product candidates are designed to be administered in a single treatment to each eye by intravitreal injection to offer patients a sustainable functional visual recovery. Developed as a treatment for Leber Hereditary Optic Neuropathy, GenSight Biologics' lead product candidate, LUMEVOQ (GS010; lenadogene nolparvovec), is currently in the review phase of its registration process in Europe, and in Phase III to move forward to a BLA filing in the US.
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